Tucson Myofilament Meeting, May 23-26

The Tucson Myofilament Meeting is an international 3.5-day Sarver Heart Center conference that brings together approximately 250 scientists focused on the structure and function of the myofilaments that comprise the contractile machinery of muscle. Spanning topics from molecular biophysics to heart and skeletal muscle disease mechanisms and drug development, the meeting is known for its highly interactive, collaborative, and informal atmosphere, with strong engagement of early career investigators.

Traditionally held biennially at the University of Wisconsin, the meeting will continue at the University of Arizona beginning in May 2026, offering a distinctive Tucson setting that fosters scientific exchange and community building.

Learn More and Register

Decoding the vascular genetic risk for heart disease

Friday, November 15, 2019 - 12:00pm
Event Location: 

Sarver Heart Center, Room 4137

Casey Romanoski, PhD

"Decoding the vascular genetic risk for heart disease"

Casey Romanoski received her undergraduate degree in Liberal Arts from the University of Arizona in 2004. She attended graduate school at UCLA where she trained in the laboratory of Dr. Jake Lusis to receive a PhD in Human Genetics in 2010. Her dissertation utilized systems genetics to elucidate mechanisms governing why endothelial cells isolated from different people exhibit differential responses to pro-inflammatory oxidized phospholipids. Next, she did post-doctoral training at UCSD in Christopher Glass’ laboratory where she focused on mechanisms whereby genetic variation among mouse strains directs differential gene regulation. Dr. Romanoski received fellowships from the NIH and American Heart Association to fund 9 out of the 10 years of her training. In 2014, Casey was awarded the NIH Pathway to Independence Award for promise as an academic researcher.  She moved to The University of Arizona as faculty in the Department of Cellular and Molecular Medicine in 2016.

The goal of Dr. Romanoski’s research program is to identify functional genetic variants, genes, mechanisms, and pathways that lead to endothelial cell (EC) dysfunction associated with inflammatory vascular diseases. Using a combination of experimental and analytical tools, the laboratory identifies relationships between genetic variants, chromatin state, and gene expression to elucidate mechanisms that govern regulatory function on the genome-wide scale.
 

Event Coordinator: 
Gilbert Maldonado
(520) 626-2000
Event Contact Department: 
Sarver Heart Center